Uitti RJ - Search Results

1

Investigating ELOVL7 coding variants in multiple system atrophy.

Wernick AI, Walton RL, Soto-Beasley AI, Koga S, Ren Y, Heckman MG, Milanowski LM, Valentino RR, Kondru N, Uitti RJ, Cheshire WP, Wszolek ZK, Dickson DW, Ross OA. Wernick AI, et al. Among authors: uitti rj. Neurosci Lett. 2021 Apr 1;749:135723. doi: 10.1016/j.neulet.2021.135723. Epub 2021 Feb 15. Neurosci Lett. 2021. PMID: 33600908 Free PMC article.

2

Western Nebraska family (family D) with autosomal dominant parkinsonism.

Wszolek ZK, Pfeiffer B, Fulgham JR, Parisi JE, Thompson BM, Uitti RJ, Calne DB, Pfeiffer RF. Wszolek ZK, et al. Among authors: uitti rj. Neurology. 1995 Mar;45(3 Pt 1):502-5. doi: 10.1212/wnl.45.3.502. Neurology. 1995. PMID: 7898705

3

Widespread alterations of alpha-synuclein in multiple system atrophy.

Dickson DW, Liu W, Hardy J, Farrer M, Mehta N, Uitti R, Mark M, Zimmerman T, Golbe L, Sage J, Sima A, D'Amato C, Albin R, Gilman S, Yen SH. Dickson DW, et al. Am J Pathol. 1999 Oct;155(4):1241-51. doi: 10.1016/s0002-9440(10)65226-1. Am J Pathol. 1999. PMID: 10514406 Free PMC article.

4

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

Wszolek ZK, Uitti RJ, Hutton M. Wszolek ZK, et al. Among authors: uitti rj. Neurology. 2000 May 23;54(10):2028-30. doi: 10.1212/wnl.54.10.2028. Neurology. 2000. PMID: 10822460 No abstract available.

5

Familial Parkinson's disease and related conditions. Clinical genetics.

Wszolek ZK, Uitti RJ, Markopoulou K. Wszolek ZK, et al. Among authors: uitti rj. Adv Neurol. 2001;86:33-43. Adv Neurol. 2001. PMID: 11553993 Review. No abstract available.

6

Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism.

Wszolek ZK, Gwinn-Hardy K, Wszolek EK, Muenter MD, Pfeiffer RF, Rodnitzky RL, Uitti RJ, McComb RD, Gasser T, Dickson DW. Wszolek ZK, et al. Among authors: uitti rj. Acta Neuropathol. 2002 Apr;103(4):344-50. doi: 10.1007/s00401-001-0474-8. Epub 2001 Dec 8. Acta Neuropathol. 2002. PMID: 11904753

7

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.

Tsuboi Y, Uitti RJ, Delisle MB, Ferreira JJ, Brefel-Courbon C, Rascol O, Ghetti B, Murrell JR, Hutton M, Baker M, Wszolek ZK. Tsuboi Y, et al. Among authors: uitti rj. Arch Neurol. 2002 Jun;59(6):943-50. doi: 10.1001/archneur.59.6.943. Arch Neurol. 2002. PMID: 12056930

8

Hereditary tauopathies and parkinsonism.

Wszolek ZK, Tsuboi Y, Farrer M, Uitti RJ, Hutton ML. Wszolek ZK, et al. Among authors: uitti rj. Adv Neurol. 2003;91:153-63. Adv Neurol. 2003. PMID: 12442674 Review. No abstract available.

9

Dopamine agonists, sleep disorders, and driving in Parkinson's disease.

Uitti RJ, Wszolek ZK. Uitti RJ, et al. Adv Neurol. 2003;91:343-9. Adv Neurol. 2003. PMID: 12442692 Review. No abstract available.

10

Magnetic resonance imaging and deep brain stimulation.

Uitti RJ, Tsuboi Y, Pooley RA, Putzke JD, Turk MF, Wszolek ZK, Witte RJ, Wharen RE Jr. Uitti RJ, et al. Neurosurgery. 2002 Dec;51(6):1423-28; discussion 1428-31. Neurosurgery. 2002. PMID: 12445347

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